Iodometry

 

To a known volume of sample, an excess but known amount of I^- is added, which the oxidizing agent then oxidizes to I₂. I₂ dissolves in the iodide-containing solution to give triiodide ions (I₃^-), which have a dark brown color. The triiodide ion solution is then titrated against standard thiosulfate solution to give iodide again using starch indicator:

I−3 + 2 e⁻ ⇌ 3 I⁻ (E⁰ = +0.54 V)

Together with reduction potential of thiosulfate:^[1]

S₄O2−6 + 2 e⁻ ⇌ 2 S₂O2−3 (E⁰ = +0.08 V)

The overall reaction is thus:

I−3 + 2 S₂O2−3 → S₄O2−6 + 3 I⁻ (E_reaction = +0.46 V)

For simplicity, the equations will usually be written in terms of aqueous molecular iodine rather than the triiodide ion, as the iodide ion did not participate in the reaction in terms of mole ratio analysis. The disappearance of the deep blue color is, due to the decomposition of the iodine-starch clathrate, marks the end point.

The reducing agent used does not necessarily need to be thiosulfate; stannous chloride, sulfites, sulfides, arsenic(III), and antimony(III) salts are commonly used alternatives^[2] at pH above 8.

At low pH, the following reaction might occur with thiosulfate:

S₂O2−3 + 2 H⁺ → SO₂ + S + H₂O

Some reactions involving certain reductants are reversible at certain pH, thus the pH of the sample solution should be carefully adjusted before performing the analysis. For example, the reaction:

H₃AsO₃ + I₂ + H₂O → H₃AsO₄ + 2 H⁺ + 2 I⁻

is reversible at pH below 4.

The volatility of iodine is also a source of error for the titration, this can be effectively prevented by ensuring an excess iodide is present and cooling the titration mixture. Strong light, nitrite and copper ions catalyse the conversion of iodide to iodine, so these should be removed prior to the addition of iodide to the sample.

For prolonged titrations, it is advised to add dry ice to the titration mixture to displace air from the Erlenmeyer flask so as to prevent the aerial oxidation of iodide to iodine. Standard iodine solution is prepared from potassium iodate and potassium iodide, which are both primary standards:

IO−3 + 8 I⁻ + 6 H⁺ → 3 I−3 + 3 H₂O

Iodine in organic solvents, such as diethyl ether and carbon tetrachloride, may be titrated against sodium thiosulfate dissolved in acetone.^{[clarification needed]}

 

Iodometry in its many variations is extremely useful in volumetric analysis. Examples include the determination of copper(II), chlorate, hydrogen peroxide, and dissolved oxygen:

2 Cu²⁺ + 4 I⁻ → 2 CuI + I₂

6 H⁺ + ClO−3 + 6 I⁻ → 3 I₂ + Cl⁻ + 3 H₂O

2 H⁺ + H₂O₂ + 2 I⁻ → I₂ + 2 H₂O

2 H₂O + 4 Mn(OH)₂ + O₂ → 4 Mn(OH)₃

2 Mn³⁺ + 2 I⁻ → I₂ + 2 Mn²⁺

Available chlorine refers to chlorine liberated by the action of dilute acids on hypochlorite. Iodometry is commonly employed to determine the active amount of hypochlorite in bleach responsible for the bleaching action. In this method, excess but known amount of iodide is added to known volume of sample, in which only the active (electrophilic) can oxidize iodide to iodine. The iodine content and thus the active chlorine content can be determined with iodometry.^[3]

The determination of arsenic(V) compounds is the reverse of the standardization of iodine solution with sodium arsenite, where a known and excess amount of iodide is added to the sample:

As₂O₅ + 4 H⁺ + 4 I⁻ ⇌ As₂O₃ + 2 I₂ + 2 H₂O

For analysis of antimony(V) compounds, some tartaric acid is added to solubilize the antimony(III) product.^[2]

Sulfites and hydrogensulfites reduce iodine readily in acidic medium to iodide. Thus when a diluted but excess amount of standard iodine solution is added to known volume of sample, the sulfurous acid and sulfites present reduces iodine quantitatively:

SO2−3 + I₂ + H₂O → SO2−4 + 2 H⁺ + 2 I⁻

HSO−3 + I₂ + H₂O → SO2−4 + 3H + + 2 I⁻

(This application is used for iodimetry titration because here iodine is directly used)

Although the sulfide content in sample can be determined straight forwardly as described for sulfites, the results are often poor and inaccurate. A better, alternative method with higher accuracy is available, which involves the addition of excess but known volume of standard sodium arsenite solution to the sample, during which arsenic trisulfide is precipitated:

As₂O₃ + 3 H₂S → As₂S₃ + 3 H₂O

The excess arsenic trioxide is then determined by titrating against standard iodine solution using starch indicator. Note that for the best results, the sulfide solution must be dilute with the sulfide concentration not greater than 0.01 M.^[2]

When iodide is added to a solution of hexacyanoferrate(III), the following equilibrium exists:

2 [Fe(CN)₆]³⁻ + 2 I⁻ ⇌ 2 [Fe(CN)₆]⁴⁻ + I₂

Under strongly acidic solution, the above equilibrium lies far to the right hand side, but is reversed in almost neutral solution. This makes analysis of hexacyanoferrate(III) troublesome as the iodide and thiosulfate decomposes in strongly acidic medium. To drive the reaction to completion, an excess amount of zinc salt can be added to the reaction mixture containing potassium ions, which precipitates the hexacyanoferrate(II) ion quantitatively:

2 [Fe(CN)₆]³⁻ + 2 I⁻ + 2 K⁺ + 2 Zn²⁺ → 2 KZn[Fe(CN)₆]⁻ + I₂

The precipitation occurs in slightly acidic medium, thus avoids the problem of decomposition of iodide and thiosulfate in strongly acidic medium, and the hexacyanoferrate(III) can be determined by iodometry as usual.^[2]

• Iodine–starch test